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Genes & Development|August 26, 2015
Noncatalytic PTEN missense mutation predisposes to organ-selective cancer development in vivoEnrico Caserta, Onur Egriboz, Hui Wang, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 11, 2023
Association of HER2DX with pathological complete response and survival outcomes in HER2-positive breast cancerG Villacampa, N M Tung, S Pernas, et al.
JAMA|March 18, 2024
Neuroimaging Findings in US Government Personnel and Their Family Members Involved in Anomalous Health IncidentsCarlo Pierpaoli, Amritha Nayak, Rakibul Hafiz, et al.
JAMA|March 18, 2024
Clinical, Biomarker, and Research Tests Among US Government Personnel and Their Family Members Involved in Anomalous Health IncidentsLeighton Chan, Mark Hallett, Chris K Zalewski, et al.
Acta Neuropathologica|January 15, 2021
Making sense of missense variants in TTN-related congenital myopathiesMartin Rees, Roksana Nikoopour, Atsushi Fukuzawa, et al.
Leukemia & Lymphoma|September 7, 2022
Development of a distributed international patient data registry for hairy cell leukemiaLeslie A Andritsos, Mirela Anghelina, Jasmine Neal, et al.
Annals of the Rheumatic Diseases|December 7, 2010
Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosisL M Diaz-Gallo, P Gourh, J Broen, et al.
NPJ Genomic Medicine|August 16, 2016
Genome-wide characteristics of de novo mutations in autismRyan K C Yuen, Daniele Merico, Hongzhi Cao, et al.
Clinical Genetics|August 19, 2015
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in careS L Sawyer, T Hartley, D A Dyment, et al.
Physical Review Letters|April 7, 2025
First Measurement of a Weak r-Process Reaction on a Radioactive NucleusM Williams, C Angus, A M Laird, et al.
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